A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6004489



Internal ID21913832
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:126145223..126149806hg38UCSC Ensembl
chr9:128907502..128912085hg19UCSC Ensembl
Cytoband9q33.3
Allele length
AssemblyAllele length
hg384584
hg194584
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17585819
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6004489
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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